Canonical Allele Identifier: CA459320842

Gene: BLK

Linked Data

• MyVariant Identifiers: chr8:g.11421509C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564000C>G , CM000670.2:g.11564000C>G	GRCh38
NC_000008.10:g.11421509C>G , CM000670.1:g.11421509C>G	GRCh37
NC_000008.9:g.11458918C>G	NCBI36
NG_023543.1:g.74989C>G
NG_023543.2:g.74989C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1518C>G
ENST00000696154.1:c.*728C>G	ENSP00000512445.1:n.*728C>G
ENST00000696155.1:n.294C>G
ENST00000259089.9:c.1410C>G MANE Select	ENSP00000259089.4:p.Ala470=
ENST00000645242.1:c.1197C>G	ENSP00000494690.1:p.Ala399=
ENST00000259089.8:c.1410C>G	ENSP00000259089.4:p.Ala470=
ENST00000526097.1:n.1350C>G
ENST00000529894.1:c.1197C>G	ENSP00000433663.1:p.Ala399=
NM_001715.2:c.1410C>G	NP_001706.2:p.Ala470=
XM_011543824.1:c.1488C>G	XP_011542126.1:p.Ala496=
XM_011543825.1:c.1488C>G	XP_011542127.1:p.Ala496=
XM_011543826.1:c.1488C>G	XP_011542128.1:p.Ala496=
XM_011543827.1:c.1275C>G	XP_011542129.1:p.Ala425=
NM_001330465.1:c.1197C>G	NP_001317394.1:p.Ala399=
XM_011543825.3:c.1488C>G	XP_011542127.1:p.Ala496=
NM_001715.3:c.1410C>G MANE Select	NP_001706.2:p.Ala470=
NM_001330465.2:c.1197C>G	NP_001317394.1:p.Ala399=